A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6449499



Internal ID21107052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:50401..211000hg38UCSC Ensembl
chr10:96341..256940hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38160600
hg19160600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv595n223
Supporting Variantsnssv18179066
Samples
Known GenesZMYND11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6449499
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer